ENST00000477226.6:n.516C>T
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|
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ENST00000683013.1:n.430C>T
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|
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ENST00000373960.4:c.1042C>T
MANE Select
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ENSP00000363071.3:p.Gln348Ter
|
|
ENST00000373960.3:c.1042C>T
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ENSP00000363071.3:p.Gln348Ter
|
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ENST00000477226.5:n.514C>T
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|
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ENST00000492726.1:n.437C>T
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NM_001927.3:c.1042C>T , LRG_380t1:c.1042C>T
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NP_001918.3:p.Gln348Ter
|
|
NM_001927.4:c.1042C>T
MANE Select
|
NP_001918.3:p.Gln348Ter
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NM_001382708.1:c.1039C>T
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NP_001369637.1:p.Gln347Ter
|
|
NM_001382709.1:c.736-126C>T
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NP_001369638.1:n.736-126C>T
|
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NM_001382710.1:c.1024-51C>T
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NP_001369639.1:n.1024-51C>T
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NM_001382711.1:c.1024-3C>T
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NP_001369640.1:n.1024-3C>T
|
|
NM_001382712.1:c.1042C>T
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NP_001369641.1:p.Gln348Ter
|
|
NM_001382713.1:c.772C>T
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NP_001369642.1:p.Gln258Ter
|
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